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Pulmonary Arterial Hypertension: Pathophysiology and Treatment

Pulmonary arterial hypertension (PAH), the first category of pulmonary hypertension, is a chronic and progressive disorder characterised by angioproliferative vasculopathy in the pulmonary arterioles, leading to endothelial and smooth muscle proliferation and dysfunction, inflammation and thrombosis...

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Dades bibliogràfiques
Publicat a:Diseases
Autors principals: Lan, Norris S. H., Massam, Benjamin D., Kulkarni, Sandeep S., Lang, Chim C.
Format: Artigo
Idioma:Inglês
Publicat: MDPI 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6023499/
https://ncbi.nlm.nih.gov/pubmed/29772649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diseases6020038
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